Charcot–Marie–Tooth disease type 2E, a disorder of the cytoskeleton von Fabrizi, Gian Maria, Cavallaro, Tiziana, Angiari, Chiara, Cabrini, Ilaria, Taioli, Federica, Malerba, Giovanni, Bertolasi, Laura, Rizzuto, Nicolo'

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Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E von FABRIZI, G. M, CAVALLARO, T, ANGIARI, C, BERTOLASI, L, CABRINI, I, FERRARINI, M, RIZZUTO, N

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Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease von FABRIZI, G. M, FERRARINI, M, CAVALLARO, T, CABRINI, I, CERINI, R, BERTOLASI, L, RIZZUTO, N

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Human Immunodeficiency Virus-Associated Peripheral Neuropathies von Ferrari, Sergio, Vento, Sandro, Monaco, Salvatore, Cavallaro, Tiziana, Cainelli, Francesca, Rizzuto, Nicolò, Temesgen, Zelalem

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The role of muscle biopsy in investigating isolated muscle pain von FILOSTO, M, TONIN, P, VATTEMI, G, BERTOLASI, L, SIMONATI, A, RIZZUTO, N, TOMELLERI, G

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Ataxia with oculomotor apraxia type 2 : A clinical, pathologic, and genetic study von CRISCUOLO, C, CHESSA, L, PIERELLI, F, RIZZUTO, N, SANTORELLI, F. M, GALLOSTI, L, FILLA, A, CASALI, C, DI GIANDOMENICO, S, MANCINI, P, SACCA, F, GRIECO, G. S, PIANE, M, BARBIERI, F, DE MICHELE, G, BANFI, S

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Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H von FABRIZI, G. M, TAIOLI, F, CAVALLARO, T, FERRARI, S, BERTOLASI, L, CASAROTTO, M, RIZZUTO, N, DECONINCK, T, TIMMERMAN, V, DE JONGHE, P

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SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION von BOARETTO, F, VETTORI, A, MOSTACCIUOLO, M. L, MARTINUZZI, A, CASARIN, A, VAZZA, G, MUGLIA, M, ROSSETTO, M. G, CAVALLARO, T, RIZZUTO, N, CARELLI, V, SALVIATI, L

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Critical illness myopathy and neuropathy von Latronico, N., Recupero, D., Candiani, A., Guarneri, B., De Maria, G., Antonini, L., Fenzi, F., Tomelleri, G., Tonin, P., Rizzuto, N.

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Natural history of CMT1A including QoL: A 2-year prospective study von Padua, L, Pareyson, D, Aprile, I, Cavallaro, T, Quattrone, A, Rizzuto, N, Vita, G, Tonali, P, Schenone, A

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Natural history of Charcot–Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life von Padua, Luca, Pareyson, D., Aprile, I., Cavallaro, T., Quattrone, D. A., Rizzuto, N., Vita, G., Tonali, P., Schenone, A.

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MELAS: clinical phenotype and morphological brain abnormalities von SPARACO, M, SIMONATI, A, CAVALLARO, T, BARTOLOMEI, L, GRAUSO, M, PISCIOLI, F, MORELLI, L, RIZZUTO, N

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Relationship between clinical examination, Quality of Life, disability and depression in CMT patients: Italian Multicenter study von Padua, L., Aprile, I., Cavallaro, T., Commodari, I., Pareyson, D., Quattrone, A., Rizzuto, N., Vita, G., Tonali, P., Schenone, A.

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Focal lesions area feature of chronic inflammatory demyelinating polyneuropathy (CIDP) von RIZZUTO, N, MORBIN, M, CAVALLARO, T, FERRARI, S, FALLAHI, M, GALIAZZO RIZZUTO, S

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Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study von Padua, L, Aprile, I, Cavallaro, T, Commodari, I, La Torre, G, Pareyson, D, Quattrone, A, Rizzuto, N, Vita, G, Tonali, P, Schenone, A

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Paired transcranial magnetic stimulation for the early diagnosis of corticobasal degeneration von Frasson, E., Bertolasi, L., Bertasi, V., Fusina, S., Bartolomei, L., Vicentini, S., Rizzuto, N., Priori, A.

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Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families von Mostacciuolo, M.L., Righetti, E., Zortea, M., Bosello, V., Schiavon, F., Vallo, L., Merlini, L., Siciliano, G., Fabrizi, G.M., Rizzuto, N., Milani, M., Baratta, S., Taroni, F.

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Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRI AA L and CMT-TRAUK): a double-blind randomised trial von Pareyson, Davide, Dr, Reilly, Mary M, Prof, Schenone, Angelo, MD, Fabrizi, Gian Maria, MD, Cavallaro, Tiziana, MD, Santoro, Lucio, Prof, Vita, Giuseppe, Prof, Quattrone, Aldo, Prof, Padua, Luca, MD, Gemignani, Franco, MD, Visioli, Francesco, PhD, Laurà, Matilde, MD, Radice, Davide, MSc, Calabrese, Daniela, MSc, Hughes, Richard AC, Prof, Solari, Alessandra, MD

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Phosphorylated 14-3-3ζ protein in the CSF of neuroleptic-treated patients von ZANUSSO, G, FIORINI, M, MONACO, S, FARINAZZO, A, GELATI, M, BENEDETTI, M. D, FERRARI, S, DALLA LIBERA, A, CAPALDI, S, MONACO, H. L, RIZZUTO, N

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A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B von FABRIZI, G. M, FERRARINI, M, CAVALLARO, T, JARRE, L, POLO, A, RIZZUTO, N

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